Visitor Monitoring Drug History: DIAMOX
 
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Label and Approval History

Drug Name: DIAMOX
FDA Application No: (NDA) 009388
Active Ingredient(s): ACETAZOLAMIDE SODIUM
Company: DURAMED PHARMS BARR
 
Label History
 
Labels are not available on this site for DIAMOX, (NDA) 009388
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/26/2002 035Control Supplement  
12/3/1999 033Control Supplement  
9/6/2000 032Manufacturing Change or Addition  
7/1/1994 031Control Supplement  
7/1/1994 030Labeling Revision  
12/9/1993 029Control Supplement  
12/13/1990 028Control Supplement  
12/5/1990 025Labeling Revision  
6/25/1954 000Approval  
 
Therapeutic Equivalents
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